(Q39945183)

15 September 2017

title

Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob disease (English)

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15 September 2017

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Katsuya Satoh

1

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15 September 2017

Minoru Tobiume

2

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15 September 2017

Yuki Matsui

3

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15 September 2017

Kazuo Mutsukura

4

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15 September 2017

Noriyuki Nishida

5

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15 September 2017

Yusei Shiga

6

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15 September 2017

Katsumi Eguhchi

7

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15 September 2017

Susumu Shirabe

8

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15 September 2017

Testutaro Sata

9

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15 September 2017

publication date

9 August 2010

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15 September 2017

published in

Laboratory Investigation

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15 September 2017

volume

90

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15 September 2017

issue

11

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15 September 2017

page(s)

1637-1644

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Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases

15 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

14-3-3 protein levels and isoform patterns in the cerebrospinal fluid of Creutzfeldt-Jakob disease patients in the progressive and terminal stages

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

7 January 2021

Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

7 January 2021

Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

7 January 2021

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

7 January 2021

14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2009.68

7 January 2021

10.1038/LABINVEST.2009.68

Identifiers

DOI

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15 September 2017

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